Design and Application of Sensors for Chemical Cytometry - ACS

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Design and Application of Sensors for Chemical Cytometry Brianna M Vickerman, Matthew M Anttila, Brae V Peterson, Nancy L Allbritton, and David S. Lawrence ACS Chem. Biol., Just Accepted Manuscript • DOI: 10.1021/acschembio.7b01009 • Publication Date (Web): 27 Jan 2018 Downloaded from http://pubs.acs.org on January 31, 2018

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ACS Chemical Biology

Design and Application of Sensors for Chemical Cytometry Brianna M. Vickerman,^† Matthew M. Anttila,^† Brae V. Peterson,^† Nancy L. Allbritton,*,†,‡,§ and David S. Lawrence*,†,§,|| †

Department of Chemistry, University of North Carolina, Chapel Hill, NC 27599, United States Joint Department of Biomedical Engineering, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599 and North Carolina State University, Raleigh, North Carolina 27695, United States § Department of Pharmacology, University of North Carolina, Chapel Hill, NC 27599, USA || Division of Chemical Biology and Medicinal Chemistry, University of North Carolina, Chapel Hill, NC 27599, USA ‡

^These authors contributed equally to the manuscript

*Corresponding Authors Nancy L. Allbritton ([email protected]) and David S. Lawrence ([email protected])

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ABSTRACT The bulk cell population response to a stimulus, be it a growth factor or a cytotoxic agent, neglects the cell-to-cell variability that can serve as a friend or as a foe in human biology. Biochemical variations amongst closely related cells furnish the basis for the adaptability of the immune system, but also acts as the root cause of resistance to chemotherapy by tumors. Consequently, the ability to probe for the presence of key biochemical variables at the single-cell level is now recognized to be of significant biological and biomedical impact. Chemical cytometry has emerged as an ultrasensitive single-cell platform with the flexibility to measure an array of cellular components, ranging from metabolite concentrations to enzyme activities. We briefly review the various chemical cytometry strategies including recent advances in reporter design, probe and metabolite separation, and detection instrumentation. We also describe strategies to improve intracellular delivery, biochemical specificity, metabolic stability, and detection sensitivity of probes. Recent applications of these strategies to small molecules, lipids, proteins, and other analytes are discussed. Finally, we assess the current scope and limitations of chemical cytometry and discuss areas for future development to meet the needs of single-cell research.


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OVERVIEW OF CHEMICAL CYTOMETRY Heterogeneity is a fundamental aspect of normal and diseased cell biology. Genetically identical cells respond differentially to an identical stimulus due to local environment conditions, varying cell states, and noise from biomolecular processes.1 Phenotype variation is not well understood, but has far reaching implications ranging from transient drug resistance in cancer to the distribution of green and red cones in a developing retina.2-4 Experiments measuring a bulk population response report the cell-averaged outcome, thereby missing variations from subpopulations, asynchronous behavior, or rare cell responses.5 Cells within a tumor are an example of cellular heterogeneity arising from both genetic and microenvironmental factors, all of which influences a cell’s response to therapeutics.5 Single-cell assays enable identification of drug-resistant cell subpopulations and even permit lineage tracing to a parental cell providing information on both clonal dynamics and drug-resistance evolution.5, 6 Immune cells likewise possess significant cell-to-cell heterogeneity, which furnishes the adaptability to protect against past and future unknown microorganisms.7 Single cell analysis, with its precision to resolve heterogeneity in cell populations, provides the means to decipher the processes behind developmental, stem, and cancer biology. Chemical cytometry is defined as the use of analytical tools to measure the composition of single cells.8, 9 This review focuses on the methods of chemical cytometry that employ chemical probes, in conjunction with a separation step, to detect analytes from single cells (Figure 1). Capillary electrophoresis (CE) is the most common separation method since the columns are well suited to handle the small volume of most cells. CE also has excellent resolving power, capable of distinguishing nearly identical species, as well as high peak capacity, enabling the simultaneous separation of many probes. CE has also been used to separate a wide variety of entities including ions, amino acids, peptides, sugars, lipids, proteins, and polynucleotides. Yoctomole detection limits (hundreds of molecules) are routinely achieved when fluorescence is used as a detection method.10 The latter requires that the target molecule is inherently fluorescent, can be derivatized with a fluorophore, or can be paired with a fluorescent reporter. Whereas image and flow cytometry require probes to be spectrally resolved, multiple probes with the same emission spectra are spatially resolved during the separation step of chemical cytometry.11, 12 Chemical cytometry as a physical process has poor intracellular spatial resolution since the entire cell must be lysed for separation and detection of targeted analytes. However, it is possible to design probes that are spatially targeted to specific intracellular sites (vide infra). By contrast, the temporal resolution of chemical cytometry is excellent, ranging from microseconds to seconds depending upon the cell-sampling method employed.13, 14 CHEMICAL CYTOMETRY, SEPARATION AND DETECTION OF REPORTERS AND ANALYTES The small amount of material in a typical mammalian cell requires an extraordinarily low limit of detection (LOD) for single-cell analysis.15 Reporter design and detection strategies must enable measurements sensitive enough to discriminate between individual cells that have small differences in analyte quantities, but robust enough to quantify large differences in concentrations within a highly heterogeneous cell population.15-17 Examples include the swings in intracellular calcium concentration observed amongst single neurons16 and the differential Akt activity between single tumor cells.17 To achieve these goals, the components of separationbased, single-cell analysis include, a cell station or holder, a separation region, and a detection



system (Figure 1). The cell holder serves as the final storage space for the cell or its contents prior to analysis. Cell holders range from the very simple i.e. Eppendorf tubes, to the more sophisticated microfabricated cell traps or microfluidic flow channels.18-22 Single living cells, fixed cells and cell lysates have all been used as inputs for chemical cytometry. Living cells can be lysed chemically, electrically, sonically or by laser cavitation just prior to or during introduction into the separation channel.23-27 The time between the initiation of lysis and the cessation of the cell's chemical reactions with the reporter is defined as the temporal resolution of the analyte’s measurement. 13, 28 Only a handful of separation and detection methods meet the stringent analytical requirements of separation based single cell analysis (Figure 2).18-22 Nonetheless, the separation step offers the advantage, relative to other single cell methods, that the probes need not be entirely specific nor undergo a change in optical properties upon binding or reaction. Multiple products and closely related molecules such as isomers can readily be distinguished in the separation step.18-22 CE, microelectrophoresis chips and nano-HPLC/ultraperformance liquid chromatography (UPLC) techniques have been used to separate species ranging in size from small molecules to macromolecules. Common detection methods for chemical cytometry include fluorescence, electrochemical detection (ED), and mass spectrometry (MS). For reporter-based chemical cytometry, fluorescence is often the preferred detection method due to its sensitivity, with LODs of as little as 1 to a few hundred molecules. However, this method of detection requires the design of a fluorescent reporter.29-31 Electrochemical detection also achieves limits approaching single molecule detection.32 However, this technique can only be used for electroactive species, and is prone to interference from electrode fouling by sample components. MS offers label free analysis since any ionizable molecule within a cell is measured. Importantly, the comparatively modest sensitivity of MS remains a significant limitation for single-cell applications, and currently limits analyses to high abundance proteins and secondary metabolites.33-36 MICROELECTROPHORESIS Electrophoretic separation of pL to µL-sized cells has been accomplished in capillaries and in channels of microdevices. These microseparation methods have been used to quantify organelle pH, proteins, peptides, lipids, gasotransmitters, small molecules and metal ions in single cells.24-27, 29, 37-48 The method employs electrokinetic separation within a small-diameter, fused-silica capillary taking advantage of the differential mobility of analyte molecules under an applied electric field..5, 21 An asset of this method is that any modification to an analyte or reporter almost always results in a new mobility under appropriate separation conditions. Fluorescence detection is typically performed on-column by interrogating the capillary with a focused light source, generally a laser, and detecting emitted light with a photomultiplier tube (PMT) or photodiode.18, 21, 26, 45 ED coupled to CE offers a multitude of advantages for single cell analysis due to its high sensitivity, low LOD, and low cost. 23, 25, 49, 50 MS coupled to CE has led to impressive advances in elucidation of the proteome and metabolome of single cells.33-36, 51 CEMS has been successfully used to characterize metabolite, and protein biomarkers within individual neurons, and single Xenopus laevis embryos respectively. In these studies protein quantitation was restricted to higher abundance species, precluding investigations of low abundance proteins which are critical in the etiology of many diseases.36, 52 In an impressive advance, Smits and colleagues have used this approach to characterize more than 5800 proteins from a single Xenopus laevis embryo, the largest single cell proteomics investigation to date.52


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Almost 10% of the characterized proteins underwent a change in abundance during early embryogenesis. Microelectrophoresis chips employing solution or gel-based separations have emerged as a viable alternative for single cell analysis.11, 27, 51, 53-61 The microchips offer significant advantages over traditional CE due to their rapid separations (ms to s), and are more amenable to parallelization due to their small footprint, and very short separation distances.22 These devices can also be interfaced with detection strategies similar to that used for CE. Herr’s group has pioneered the development of microelectrophoresis chips for gel-based separations of proteins from single cells for immunoblotting and western blotting-based assays. This type of analysis supports multiplexing of up to 12 proteins.62 Numerous opportunities remain for the development of microelectrophoresis devices for single cell assays since other components such as valves, pumps, electrodes, fiber optics, and other functionalities can be fully integrated into the devices.22 LIQUID CHROMATOGRAPHY High performance liquid chromatography (HPLC) utilizes an analyte’s differential partitioning in a liquid mobile phase and a stationary phase to accomplish separation.63 In ground breaking work, Kennedy and Jorgenson quantified neurotransmitters within Helix aspersa neurons using open tubular dimethyloctadecylsilane reverse phase-HPLC with electrochemical detection in the 1980's.63 Since then, the majority of more recent LC-based, single-cell assays have used MS for detection. While a powerful method, LC-MS assays of single cells are largely restricted to very large-sized cells such as Xenopus laevis embryo cells and/or high-concentration analytes including, abundant proteins (basal transcription factors), toxic secondary metabolites (diarrheic shellfish toxins produced by the Dinophysis genus), and plant pigments (anthocyanins).52, 64, 65 Hen et al. recently loaded 100 living cells into a sample loop for simultaneous lysis, protein digestion and assay by LC-MS lowering detection limits to identify 600 distinct proteins.66 Thus while LC-MS still does not reach the needed sensitivity for cytometry of most analytes in single mammalian cells, progress is exciting and will undoubtedly enable new biologic insights. REPORTER DESIGN ELEMENTS Effective reporters of intracellular biochemical processes must display a multitude of traits, including the ability to (1) penetrate the plasma membrane, (2) distinguish between closely related biochemical events, (3) retain structural integrity in the metabolically active intracellular environment, (4) control when (and/or where) the measurements are acquired, and (5) provide an exquisitely sensitive readout. Furthermore, the design strategies must be functionally adaptable to accommodate the diverse array of analytes that have attracted biological and biomedical interest, including metal ions, gases, metabolites, hormones, and enzymes. Cell Permeability. There are a variety of physical and chemical strategies to introduce membrane impermeable agents into the cytoplasm of target cells. However, physical methods, such as microinjection or electroporation damage the plasma membrane and activate cell repair pathways. By contrast, cytoplasmic access via passive diffusion is the ideal form of cellular entry. Probes that are small molecules or peptides have a better chance at crossing the lipid bilayer if they are lipophilic, relatively small in size, and do not have significantly polar groups.67



However, the requisite traits of an effective intracellular reporter may preclude ready membrane permeability. Under these circumstances, various covalent accessories can be appended to the reporter such as cell penetrating peptides (CPPs)68, 69 or lipids70, 71. A disulfide bridge is commonly inserted between the reporter and the lipophilic auxiliary group. Upon entry into the cell, the high intracellular glutathione content subsequently reduces the disulfide, thereby separating the reporter by its membrane-permeant accessory. Alternatively, hydrophobic lightcleavable “caging” groups have been used to assist in transporting membrane-impermeant reporters into the cell.72 Unfortunately, none of these methods is universally applicable. The efficacy of any of these agents can be difficult to predict as it depends on the unique structural characteristics of cell impermeable agent. Selectivity and Stability. Reporter selectivity for the analyte can be an extremely challenging problem, whether it’s distinguishing between structurally similar small molecules or catalytically similar enzymes. For example, the substrate specificity of some protein kinases is virtually identical. On the other hand, in many disorders, the activity of certain protein kinases is dramatically upregulated, enabling selective detection of the target kinase even though the reporter displays less than absolute selectivity. In short, the quest for reporter selectivity for a given target, while daunting, depends upon the circumstances and is not insurmountable. An equally important issue, however, is validation of probe selectivity within the complex intracellular milieu. Methods that attenuate or accentuate probe readout are the most direct approach, and include inhibitors or activators for target enzymes, chelators for or delivery of target ions, and knock-downs or knock-ins of proteins in biochemical pathways that generate the target analyte. The intracellular milieu can be an exceptionally unfriendly place for xenobiotics. A case in point is peptides, which can contain amide bonds (especially those involving Arg and Lys residues)31, 73 prone to intracellular proteases. Although the intracellular lifespan of peptides can be enhanced via the application of protease inhibitors, disrupting key protease targets, like the proteasome, can have unintended consequences that could compromise biochemical measurements. A more useful alternative to the application of protease inhibitors is the preparation of peptide-based probes that are resistant to protease action. A number of strategies have been applied, including the introduction of unnatural residues, such as D-amino acids or Nmethyl derivatives, at proteolytically sensitive sites.31, 73 Alternatively, cytosolic proteases typically have a narrow tunnel or deep cleft that leads to the active site and the N-terminus of peptides enter this tunnel to be degraded. Consequently, protease resistance can be conferred by modifying the peptide’s N-terminus so that it is unable to access the catalytic cleft.74 Finally, peptide “stapling” and cyclization have been used to promote peptide stability in cytosolic environments. The “staple” is a covalent bond between two residues that enforces the α-helicity of a peptide, which can enhance both protease resistance and cell permeability. However, the rigid secondary structure of stapled peptides can be inconsistent with many protein-processing enzymes, including protein kinases and protein phosphatases. Indeed, the introduction of structural modifications to resist proteolysis must be performed with care so as not to interfere with the intended biological measurement. An especially insidious example of the hostile intracellular environment faced by biochemical probes is the presence of protein tyrosine phosphatases (PTPases). PTPases catalyze the hydrolysis of phosphate monoesters, which can interfere with probes designed to assess protein kinase activity. This is especially troublesome with protein tyrosine kinase (PTKs). In this regard, peptide-based PTK reporters containing a


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constrained tyrosine (1) analog, 7-(S)-hydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (L-Htc; 2), serve as effective PTK substrates (cf. 1 and 2). In addition, the nature of the constraint dramatically reduces the susceptibility of the phosphorylated product to phosphatasecatalyzed hydrolysis while enhancing the proteolytic resistance of the peptide.75

Temporal and Spatial Control. Loading active reporters into cells can result in varying times that the reporters are exposed to the analyte or enzyme under study. This is not necessarily a problem if the final readout is simply the measurement of an equilibrium condition (e.g. assessing the presence of a metal ion) or if following loading, a biochemical event is initiated by the application of triggering event (e.g. antibody binding to a receptor). However, it may be useful to probe the biochemistry of resting cells, such as in the case of diseased cells obtained from patients. Furthermore, the acquisition of well-defined kinetics requires well-defined start points. These needs can be addressed by employing light-activated reporters, which can be loaded into cells and subsequently activated with high temporal resolution when needed.72 Finally, we note that general measurements throughout the cytoplasm only provide an averaged assessment of biochemical activity. The biochemistry of the cell is highly compartmentalized, resulting in biochemical events at different intracellular sites. However, it is possible to localize probes at specific sites within a cell using compartment-targeted small molecules or specific amino acid sequences. CLASSES OF BIOCHEMICAL MEASUREMENTS A variety of analytes have been measured using chemical cytometry, including metal ions, gases, small molecule metabolites, nucleic acids, hormones, and enzymatic activity (Figure 3). These species, which vary in molecular weight from less than 50 g/mol to over 50,000 g/mol, can be detected at levels as little as 10-21 moles (Figure 4). Detection of Small Molecules. Two different strategies have been utilized to assay small molecules within or secreted by single cells, reactive fluorescent probes and reversibly binding fluorescent reporters. In the first strategy, reactive probes incorporating a fluorophore convert a nonfluorescent or fluorescent analyte into a fluorescent product(s). This product is then readily identified during a separation step based on its characteristic migration time and quantified from its fluorescence intensity. An advantage of chemical cytometry is that the reactive probe does not need to be entirely specific since the various product forms are readily separated and identified.11, 12 This strategy has been used with great success to detect various nitrogen species as well as reactive oxygen species (ROS). Nitric oxide (NO), a second messenger participating in a range of cellular processes e.g. neural transmission and immune response is commonly detected using a diamino-quenched fluorophore that becomes fluorescent upon reaction with NO.11, 38, 45, 76, 77 Additional reducing species also react with these probes to yield fluorescent products that are separated and identified by CE. Rhodamine, BODIPY, and fluorescein are commonly used fluorophores and a comparison of the different probes and their applications have been covered by Ye et. al.78 The probe can also be chemically engineered to tailor it for the



specific study requirements. For example, Zhang et. al. created the water soluble diamino BODIPY probe 3 by adding sulfonate groups so that both extracellular and intracellular NO (4) of a trapped cell can be measured before and after lysis.79

ROS are involved in inflammation, aging and cancer, and are produced by mitochondria and intracellular enzymes (e.g. NADPH oxidase).80 ROS are also used a signaling molecule within cells, for example in EGFR tyrosine phosphorylation.80 A strength of chemical cytometry is high efficiency separation, which enables multiple probe products to be quantified from the same single cell to track multiple steps within the ROS pathway.39, 76, 81 Superoxide anion (O2·-) and NO were simultaneously detected by reaction with the 1,3-dibenzothiazolinecyclohexene derivative (5 7) and 3-amino,4-aminomethyl-2,7-difluorescein diacetate (6 8), respectively, which helped to elucidate the role of O2·- in altering NO levels in neural cells exposed to stimulants.76 The separation step also enables analytes and internal standards to be

simultaneously used for greater accuracy in quantitation. Superoxide production in skeletal muscle tissues can be measured using triphenylphosphonium hydroethidine (9 10) when paired with unreactive rhodamine 123 as an internal standard. Thus accumulation of the reporter within mitochondria membranes can be tracked at varying membrane potentials.39, 40


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A key feature of chemical cytometry is that promiscuous probes, which are generally more easily designed than highly specific probes, are assets enabling simultaneous measurement of multiple reactions since the separation step compensates for the lack of probe specificity. Antioxidants such as glutathione and cysteine, play a role in mitigating ROS impacts and are measured using a single cyanine dye (11) to react with both glutathione and cysteine to form fluorescent species at 805 and 755 nm, respectively.27 When combined with the sulfonated fluorescein probe 14, hydrogen peroxide can be simultaneously measured at 525 nm.27

The flexibility provided by separations in chemical cytometry has been used to measure a diverse range of molecular species, including ions (Na+, K+, Ca2+, Mg2+),48 small molecules (amino acids, taurine),82 and small proteins83. An additional advantage of chemical cytometry over other single-cell assays is the ability to implement competitive assays within the separation device. Insulin secreted from islet cells was quantified in a microfluidic device by co-injecting the cell secretate with fluorescein-tagged insulin, and anti-insulin antibodies followed by measurement of the ratio of unbound fluorescein-insulin to antibody-bound fluorescein-insulin to quantify secreted insulin.83 This competitive detection achieved a temporal resolution of 10 s to follow glucose-responsive insulin secretion over time and should be applicable to a multitude of other hormones.14 Lipids/Lipid Kinases. Lipids encompass a diverse array of compounds that perform numerous functions within mammalian cells including, serving as structural components of cell membranes, energy storage sources, and intra/inter-cellular signaling molecules. The diverse nature of lipid function is a direct consequence of their high degree of structural heterogeneity, which arises from the numerous biosynthetic transformations available to acetyl, propionyl, and isoprene lipid precursors. Eight classes of lipids are produced in eukaryotic cells, fatty acyl



lipids, glycerolipids, glycerophospholipids, sphingolipids, saccharolipids, polyketides, sterol lipids, and prenol lipids.84 Although lipids are ubiquitous chemical components of mammalian cells, numerous challenges exist for the analysis of signaling lipids at the single cell level, (1) extremely low intracellular concentrations of signaling lipids (

Design and Application of Sensors for Chemical Cytometry - ACS

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